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Heterozygous 17-bp deletion in the forkhead transcription factor gene,FOXL2, in a Japanese family with blepharophimosis-ptosis-epicanthus inversus syndrome

✍ Scribed by T. Yamada; S. Hayasaka; M. Matsumoto; Budu; T. Esa; Y. Hayasaka; M. Endo


Book ID
106252635
Publisher
Nature Publishing Group
Year
2001
Tongue
English
Weight
981 KB
Volume
46
Category
Article
ISSN
1435-232X

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